Literature DB >> 26671972

Longitudinal plasma metanephrines preceding pheochromocytoma diagnosis: a retrospective case-control serum repository study.

S W Olson, S Yoon, T Baker1, L K Prince, D Oliver, K C Abbott1.   

Abstract

OBJECTIVE: Plasma metanephrines (PMN) are highly sensitive for diagnosis of pheochromocytoma, but the natural history of PMN before pheochromocytoma diagnosis has not been previously described. The aim of the study was to compare the progression of PMN before pheochromocytoma diagnosis to matched healthy and essential hypertension disease controls.
DESIGN: A retrospective case-control Department of Defense Serum Repository (DoDSR) study.
METHODS: We performed a DoDSR study that compared three longitudinal pre-diagnostic PMN for 30 biopsy-proven pheochromocytoma cases to three longitudinal PMN for age, sex, race, and age of serum sample matched healthy and essential hypertension disease controls. Predominant metanephrine (MN) or normetanephrine (NMN) production was identified for each case and converted to a percentage of the upper limit of normal to allow analysis of all cases together. PMN were measured by Quest Diagnostics.
RESULTS: The predominant plasma metanephrine (PPM) was >100 and 300% of the upper limit of normal a median of 6.6 and 4.1 years before diagnosis respectively. A greater percentage of pheochromocytoma patients had a PPM >100 and >300% of the upper limit of normal compared with combined healthy and essential hypertension disease controls <2, 2-8, and >8 years prior to diagnosis. For patients with a baseline PPM 90-300% of the upper limit of normal, a 25% rate of rise per year was 100% specific for pheochromocytoma.
CONCLUSIONS: PPMs elevate years before diagnosis which suggests that delayed diagnoses are common. For mild PMN elevations, follow-up longitudinal PMN trends may provide a highly specific and economical diagnostic tool.
© 2016 European Society of Endocrinology.

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Year:  2015        PMID: 26671972     DOI: 10.1530/EJE-15-0651

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  9 in total

1.  PHEOCHROMOCYTOMA CONCEALED BY CHRONIC METHAMPHETAMINE ABUSE.

Authors:  Georgiana Constantinescu; Steffen Leike; Matthias Gruber; Katharina Langton; Carola Kunath; Mirko Peitzsch; Jaap Deinum; Graeme Eisenhofer; Jacques Lenders
Journal:  AACE Clin Case Rep       Date:  2020-09-21

2.  Comparison of plasma metanephrines in patients with cyanotic and acyanotic congenital heart disease.

Authors:  Mojca Jensterle; Ana Podbregar; Andrej Janež; Matej Rakusa; Katja Goricar; Katja Prokšelj
Journal:  Endocrine       Date:  2022-10-04       Impact factor: 3.925

3.  Adrenocortical Tumors and Pheochromocytoma/Paraganglioma Initially Mistaken as Neuroblastoma-Experiences From the GPOH-MET Registry.

Authors:  Michaela Kuhlen; Christina Pamporaki; Marina Kunstreich; Stefan A Wudy; Michaela F Hartmann; Mirko Peitzsch; Christian Vokuhl; Guido Seitz; Michael C Kreissl; Thorsten Simon; Barbara Hero; Michael C Frühwald; Peter Vorwerk; Antje Redlich
Journal:  Front Endocrinol (Lausanne)       Date:  2022-06-17       Impact factor: 6.055

4.  Characteristics of Pediatric vs Adult Pheochromocytomas and Paragangliomas.

Authors:  Christina Pamporaki; Barbora Hamplova; Mirko Peitzsch; Aleksander Prejbisz; Felix Beuschlein; Henri J L M Timmers; Martin Fassnacht; Barbara Klink; Maya Lodish; Constantine A Stratakis; Angela Huebner; Stephanie Fliedner; Mercedes Robledo; Richard O Sinnott; Andrzej Januszewicz; Karel Pacak; Graeme Eisenhofer
Journal:  J Clin Endocrinol Metab       Date:  2017-04-01       Impact factor: 5.958

Review 5.  Current Management of Pheochromocytoma/Paraganglioma: A Guide for the Practicing Clinician in the Era of Precision Medicine.

Authors:  Svenja Nölting; Martin Ullrich; Jens Pietzsch; Christian G Ziegler; Graeme Eisenhofer; Ashley Grossman; Karel Pacak
Journal:  Cancers (Basel)       Date:  2019-10-08       Impact factor: 6.639

Review 6.  Pediatric Metastatic Pheochromocytoma and Paraganglioma: Clinical Presentation and Diagnosis, Genetics, and Therapeutic Approaches.

Authors:  Mickey J M Kuo; Matthew A Nazari; Abhishek Jha; Karel Pacak
Journal:  Front Endocrinol (Lausanne)       Date:  2022-07-12       Impact factor: 6.055

Review 7.  Biochemical Diagnosis of Catecholamine-Producing Tumors of Childhood: Neuroblastoma, Pheochromocytoma and Paraganglioma.

Authors:  Graeme Eisenhofer; Mirko Peitzsch; Nicole Bechmann; Angela Huebner
Journal:  Front Endocrinol (Lausanne)       Date:  2022-07-26       Impact factor: 6.055

8.  REMISSION OF LONGSTANDING INSULIN-TREATED DIABETES MELLITUS FOLLOWING SURGICAL RESECTION OF PHEOCHROMOCYTOMA.

Authors:  Owain M Leng; Asgar C Madathil
Journal:  AACE Clin Case Rep       Date:  2019-01-30

9.  Multidisciplinary practice guidelines for the diagnosis, genetic counseling and treatment of pheochromocytomas and paragangliomas.

Authors:  R Garcia-Carbonero; F Matute Teresa; E Mercader-Cidoncha; M Mitjavila-Casanovas; M Robledo; I Tena; C Alvarez-Escola; M Arístegui; M R Bella-Cueto; C Ferrer-Albiach; F A Hanzu
Journal:  Clin Transl Oncol       Date:  2021-05-06       Impact factor: 3.405

  9 in total

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